{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,14]],"date-time":"2026-05-14T16:35:15Z","timestamp":1778776515107,"version":"3.51.4"},"reference-count":28,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2018,12,11]],"date-time":"2018-12-11T00:00:00Z","timestamp":1544486400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"DOI":"10.13039\/100004339","name":"Sanofi","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100004339","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Transfusion"],"published-print":{"date-parts":[[2019,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Plerixafor (PFX) mobilizes CD34+ cells into circulation by disrupting the CXCR4 binding of the hematopoietic stem cell in its bone marrow niche.<\/jats:p><\/jats:sec><jats:sec><jats:title>Study design and Methods<\/jats:title><jats:p>in the prospective HOVON\u2010107 study (<jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"http:\/\/www.hovon.nl\">www.hovon.nl<\/jats:ext-link>) 23 allogeneic HLA\u2013identical sibling donors received one or two subcutaneous (sc) injections of plerixafor 0.320 mg\/kg.The primary endpoint, was defined as feasibility to mobilize a minimum of 2.0 x10<jats:sup>6<\/jats:sup> CD34+ cells\/kg recipient weight obtained by leukopheresis in at least 90% of the donors.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>median 3.3 x 10<jats:sup>6<\/jats:sup> CD34<jats:sup>+<\/jats:sup> cells\/kg (1.9\u20106.5) were collected after 1 (n=12) or 2 (n=10) sc injections of PFX. Side effects occurred in 15\/23 (65%) donors: most were grade 1\u20102; in 5 donors grade 3 and all resolved. All grafts were directly transplanted. Compared to 10 grafts obtained with G\u2010CSF the number of CD34+ cells was 2.4 fold lower but the percentage of phenotypically most immature CD34+ subset was higher (31% vs 15%). The total number of CD3+ cells in the graft seemed higher after PFX\u2010mobilization, but CD4\/CD 8 ratios, and frequencies of Th2, Th17 and regulatory T\u2010cells or NK cells were comparable. All patients engrafted and no increase in incidence or severity of acute or chronic graft versus host disease was observed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>stem cell mobilization with sc PFX 0.320 mg\/kg in allogeneic sibling donors is feasible with limited toxicity for donors. 14 allogeneic donors were mobilized with PFX 0.320 mg intravenously according to the same protocol. Due to the limited numbers, these results are in the supplementary section.<\/jats:p><\/jats:sec>","DOI":"10.1111\/trf.15037","type":"journal-article","created":{"date-parts":[[2018,12,12]],"date-time":"2018-12-12T04:45:35Z","timestamp":1544589935000},"page":"316-324","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":17,"title":["The feasibility and efficacy of subcutaneous plerixafor for mobilization of peripheral blood stem cells in allogeneic HLA\u2013identical sibling donors: results of the HOVON\u2010107 study"],"prefix":"10.1111","volume":"59","author":[{"given":"Georgine E.","family":"de Greef","sequence":"first","affiliation":[{"name":"Department of Hematology Erasmus MC Cancer Institute  Rotterdam Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eric","family":"Braakman","sequence":"additional","affiliation":[{"name":"Department of Hematology Erasmus MC Cancer Institute  Rotterdam Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bronno","family":"van der Holt","sequence":"additional","affiliation":[{"name":"Department of Hematology HOVON Data Center. Erasmus MC  Rotterdam Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jeroen J.W.M.","family":"Janssen","sequence":"additional","affiliation":[{"name":"Department of Hematology VU University Hospital  Amsterdam Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eefke","family":"Petersen","sequence":"additional","affiliation":[{"name":"Department of Hematology UMC Utrecht  Utrecht Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vladimir","family":"Vucinic","sequence":"additional","affiliation":[{"name":"Department of Hematology, Clinical Oncology and Hemostaseology University of Leipzig  Leipzig Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nicole","family":"Thuss","sequence":"additional","affiliation":[{"name":"Department of Hematology HOVON Data Center. 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